Prognostic significance of delayed intraventricular haemorrhage in the INTERACT studies.
Identifieur interne : 001389 ( PubMed/Corpus ); précédent : 001388; suivant : 001390Prognostic significance of delayed intraventricular haemorrhage in the INTERACT studies.
Auteurs : Tom J. Moullaali ; Shoichiro Sato ; Xia Wang ; Alejandro A. Rabinstein ; Hisatomi Arima ; Cheryl Carcel ; Guofang Chen ; Thompson Robinson ; Emma Heeley ; Edward Chan ; Candice Delcourt ; Christian Stapf ; Charlotte Cordonnier ; Richard I. Lindley ; John Chalmers ; Craig S. AndersonSource :
- Journal of neurology, neurosurgery, and psychiatry [ 1468-330X ] ; 2017.
English descriptors
- KwdEn :
- Aged, Cerebral Hemorrhage (complications), Cerebral Hemorrhage (diagnosis), Cerebral Hemorrhage (diagnostic imaging), Cerebral Hemorrhage (mortality), Cerebral Ventricles (blood supply), Cerebral Ventricles (diagnostic imaging), Disability Evaluation, Female, Hemorrhage (complications), Hemorrhage (diagnosis), Hemorrhage (diagnostic imaging), Hemorrhage (mortality), Humans, Magnetic Resonance Imaging, Male, Neuroimaging, Prognosis, Randomized Controlled Trials as Topic, Time Factors.
- MESH :
- blood supply : Cerebral Ventricles.
- complications : Cerebral Hemorrhage, Hemorrhage.
- diagnosis : Cerebral Hemorrhage, Hemorrhage.
- diagnostic imaging : Cerebral Hemorrhage, Cerebral Ventricles, Hemorrhage.
- mortality : Cerebral Hemorrhage, Hemorrhage.
- Aged, Disability Evaluation, Female, Humans, Magnetic Resonance Imaging, Male, Neuroimaging, Prognosis, Randomized Controlled Trials as Topic, Time Factors.
Abstract
Intraventricular extension of intracerebral haemorrhage (ICH) predicts poor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined. We determined the prognostic significance of dIVH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT 1 and 2).
DOI: 10.1136/jnnp-2015-311562
PubMed: 26746184
Links to Exploration step
pubmed:26746184Le document en format XML
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Moullaali</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Sato, Shoichiro" sort="Sato, Shoichiro" uniqKey="Sato S" first="Shoichiro" last="Sato">Shoichiro Sato</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Xia" sort="Wang, Xia" uniqKey="Wang X" first="Xia" last="Wang">Xia Wang</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Rabinstein, Alejandro A" sort="Rabinstein, Alejandro A" uniqKey="Rabinstein A" first="Alejandro A" last="Rabinstein">Alejandro A. 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Anderson</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2017">2017</date><idno type="RBID">pubmed:26746184</idno><idno type="pmid">26746184</idno><idno type="doi">10.1136/jnnp-2015-311562</idno><idno type="wicri:Area/PubMed/Corpus">001389</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001389</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Prognostic significance of delayed intraventricular haemorrhage in the INTERACT studies.</title><author><name sortKey="Moullaali, Tom J" sort="Moullaali, Tom J" uniqKey="Moullaali T" first="Tom J" last="Moullaali">Tom J. Moullaali</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Sato, Shoichiro" sort="Sato, Shoichiro" uniqKey="Sato S" first="Shoichiro" last="Sato">Shoichiro Sato</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Wang, Xia" sort="Wang, Xia" uniqKey="Wang X" first="Xia" last="Wang">Xia Wang</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Rabinstein, Alejandro A" sort="Rabinstein, Alejandro A" uniqKey="Rabinstein A" first="Alejandro A" last="Rabinstein">Alejandro A. Rabinstein</name><affiliation><nlm:affiliation>Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.</nlm:affiliation></affiliation></author><author><name sortKey="Arima, Hisatomi" sort="Arima, Hisatomi" uniqKey="Arima H" first="Hisatomi" last="Arima">Hisatomi Arima</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Carcel, Cheryl" sort="Carcel, Cheryl" uniqKey="Carcel C" first="Cheryl" last="Carcel">Cheryl Carcel</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Chen, Guofang" sort="Chen, Guofang" uniqKey="Chen G" first="Guofang" last="Chen">Guofang Chen</name><affiliation><nlm:affiliation>Department of Neurology, Xuzhou Central Hospital, Jiangsu, China.</nlm:affiliation></affiliation></author><author><name sortKey="Robinson, Thompson" sort="Robinson, Thompson" uniqKey="Robinson T" first="Thompson" last="Robinson">Thompson Robinson</name><affiliation><nlm:affiliation>Department of Cardiovascular Sciences and NIHR Biomedical Research Unit for Cardiovascular Diseases, University of Leicester, Leicester, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Heeley, Emma" sort="Heeley, Emma" uniqKey="Heeley E" first="Emma" last="Heeley">Emma Heeley</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Chan, Edward" sort="Chan, Edward" uniqKey="Chan E" first="Edward" last="Chan">Edward Chan</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Delcourt, Candice" sort="Delcourt, Candice" uniqKey="Delcourt C" first="Candice" last="Delcourt">Candice Delcourt</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Stapf, Christian" sort="Stapf, Christian" uniqKey="Stapf C" first="Christian" last="Stapf">Christian Stapf</name><affiliation><nlm:affiliation>Department of Neurology, CRCHUM, APHP-Hôpital Lariboisière, Paris, France.</nlm:affiliation></affiliation></author><author><name sortKey="Cordonnier, Charlotte" sort="Cordonnier, Charlotte" uniqKey="Cordonnier C" first="Charlotte" last="Cordonnier">Charlotte Cordonnier</name><affiliation><nlm:affiliation>University of Lille, CHRU, INSERM U 1171, Lille, France.</nlm:affiliation></affiliation></author><author><name sortKey="Lindley, Richard I" sort="Lindley, Richard I" uniqKey="Lindley R" first="Richard I" last="Lindley">Richard I. Lindley</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Chalmers, John" sort="Chalmers, John" uniqKey="Chalmers J" first="John" last="Chalmers">John Chalmers</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Anderson, Craig S" sort="Anderson, Craig S" uniqKey="Anderson C" first="Craig S" last="Anderson">Craig S. Anderson</name><affiliation><nlm:affiliation>The George Institute for Global Health, Sydney, Australia.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Journal of neurology, neurosurgery, and psychiatry</title><idno type="eISSN">1468-330X</idno><imprint><date when="2017" type="published">2017</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Cerebral Hemorrhage (complications)</term><term>Cerebral Hemorrhage (diagnosis)</term><term>Cerebral Hemorrhage (diagnostic imaging)</term><term>Cerebral Hemorrhage (mortality)</term><term>Cerebral Ventricles (blood supply)</term><term>Cerebral Ventricles (diagnostic imaging)</term><term>Disability Evaluation</term><term>Female</term><term>Hemorrhage (complications)</term><term>Hemorrhage (diagnosis)</term><term>Hemorrhage (diagnostic imaging)</term><term>Hemorrhage (mortality)</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Neuroimaging</term><term>Prognosis</term><term>Randomized Controlled Trials as Topic</term><term>Time Factors</term></keywords><keywords scheme="MESH" qualifier="blood supply" xml:lang="en"><term>Cerebral Ventricles</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Cerebral Hemorrhage</term><term>Hemorrhage</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Cerebral Hemorrhage</term><term>Hemorrhage</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Cerebral Hemorrhage</term><term>Cerebral Ventricles</term><term>Hemorrhage</term></keywords><keywords scheme="MESH" qualifier="mortality" xml:lang="en"><term>Cerebral Hemorrhage</term><term>Hemorrhage</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Disability Evaluation</term><term>Female</term><term>Humans</term><term>Magnetic Resonance Imaging</term><term>Male</term><term>Neuroimaging</term><term>Prognosis</term><term>Randomized Controlled Trials as Topic</term><term>Time Factors</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Intraventricular extension of intracerebral haemorrhage (ICH) predicts poor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined. We determined the prognostic significance of dIVH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT 1 and 2).</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26746184</PMID><DateCreated><Year>2016</Year><Month>01</Month><Day>09</Day></DateCreated><DateCompleted><Year>2017</Year><Month>05</Month><Day>25</Day></DateCompleted><DateRevised><Year>2017</Year><Month>11</Month><Day>14</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1468-330X</ISSN><JournalIssue CitedMedium="Internet"><Volume>88</Volume><Issue>1</Issue><PubDate><Year>2017</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Journal of neurology, neurosurgery, and psychiatry</Title><ISOAbbreviation>J. Neurol. Neurosurg. Psychiatry</ISOAbbreviation></Journal><ArticleTitle>Prognostic significance of delayed intraventricular haemorrhage in the INTERACT studies.</ArticleTitle><Pagination><MedlinePgn>19-24</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1136/jnnp-2015-311562</ELocationID><Abstract><AbstractText Label="BACKGROUND AND PURPOSE" NlmCategory="OBJECTIVE">Intraventricular extension of intracerebral haemorrhage (ICH) predicts poor outcome, but the significance of delayed intraventricular haemorrhage (dIVH) is less well defined. We determined the prognostic significance of dIVH in the Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trials (INTERACT 1 and 2).</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Pooled analyses of the INTERACT CT substudies-international, multicentre, prospective, open, blinded end point, randomised controlled trials of patients with acute spontaneous ICH and elevated systolic blood pressure (SBP)-randomly assigned to intensive (<140 mm Hg) or guideline-based (<180 mm Hg) SBP management. Participants had blinded central analyses of baseline and 24 h CTs, with dIVH defined as new intraventricular haemorrhage (IVH) on the latter scan. Outcomes of death and major disability were defined by modified Rankin Scale scores at 90 days.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">There were 349 (27%) of 1310 patients with baseline IVH, and 107 (11%) of 961 initially IVH-free patients who developed dIVH. Significant associations of dIVH were prior warfarin anticoagulation, high (≥15) baseline National Institutes of Health Stroke Scale score, larger (≥15 mL) ICH volume, greater ICH growth and higher achieved SBP over 24 h. Compared with those who were IVH-free, dIVH had greater odds of 90-day death or major disability versus initial IVH (adjusted ORs 2.84 (95% CI 1.52 to 5.28) and 1.87 (1.36 to 2.56), respectively (p trend <0.0001)).</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Although linked to factors determining greater ICH growth including poor SBP control, dIVH is independently associated with poor outcome in acute small to moderate-size ICH.</AbstractText><AbstractText Label="TRIAL REGISTRATION NUMBERS" NlmCategory="UNASSIGNED">NCT00226096 and NCT00716079.</AbstractText><CopyrightInformation>Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Moullaali</LastName><ForeName>Tom J</ForeName><Initials>TJ</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sato</LastName><ForeName>Shoichiro</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Xia</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rabinstein</LastName><ForeName>Alejandro A</ForeName><Initials>AA</Initials><AffiliationInfo><Affiliation>Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Arima</LastName><ForeName>Hisatomi</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Center for Epidemiologic Research in Asia, Shiga University of Medical Sciences, Shiga, Japan.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Carcel</LastName><ForeName>Cheryl</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>Guofang</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Department of Neurology, Xuzhou Central Hospital, Jiangsu, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Robinson</LastName><ForeName>Thompson</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Department of Cardiovascular Sciences and NIHR Biomedical Research Unit for Cardiovascular Diseases, University of Leicester, Leicester, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Heeley</LastName><ForeName>Emma</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chan</LastName><ForeName>Edward</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Delcourt</LastName><ForeName>Candice</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Neurology Department, Royal Prince Alfred Hospital, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Stapf</LastName><ForeName>Christian</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Department of Neurology, CRCHUM, APHP-Hôpital Lariboisière, Paris, France.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Département de Neurosciences, Université de Montréal, Montréal, Quebec, Canada.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Cordonnier</LastName><ForeName>Charlotte</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>University of Lille, CHRU, INSERM U 1171, Lille, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lindley</LastName><ForeName>Richard I</ForeName><Initials>RI</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Westmead Hospital Clinical School, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chalmers</LastName><ForeName>John</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Anderson</LastName><ForeName>Craig S</ForeName><Initials>CS</Initials><AffiliationInfo><Affiliation>The George Institute for Global Health, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Sydney Medical School, The University of Sydney, Sydney, Australia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Neurology Department, Royal Prince Alfred Hospital, Sydney, Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><CollectiveName>INTERACT Investigators</CollectiveName></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>ClinicalTrials.gov</DataBankName><AccessionNumberList><AccessionNumber>NCT00226096</AccessionNumber><AccessionNumber>NCT00716079</AccessionNumber></AccessionNumberList></DataBank></DataBankList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016448">Multicenter Study</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2016</Year><Month>01</Month><Day>08</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>J Neurol Neurosurg Psychiatry</MedlineTA><NlmUniqueID>2985191R</NlmUniqueID><ISSNLinking>0022-3050</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002543" MajorTopicYN="N">Cerebral Hemorrhage</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002552" MajorTopicYN="N">Cerebral Ventricles</DescriptorName><QualifierName UI="Q000098" MajorTopicYN="Y">blood supply</QualifierName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004185" MajorTopicYN="N">Disability Evaluation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006470" MajorTopicYN="N">Hemorrhage</DescriptorName><QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName><QualifierName UI="Q000175" MajorTopicYN="Y">diagnosis</QualifierName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000401" MajorTopicYN="N">mortality</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008279" MajorTopicYN="N">Magnetic Resonance Imaging</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D059906" MajorTopicYN="N">Neuroimaging</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011379" MajorTopicYN="N">Prognosis</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016032" MajorTopicYN="N">Randomized Controlled Trials as Topic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate 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